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Regulation of Chemokines and Cytokines by Histone Deacetylases and an Update on Histone Decetylase Inhibitors in Human Diseases

机译:组蛋白去乙酰化酶对趋化因子和细胞因子的调节及人类疾病中组蛋白去甲酰化酶抑制剂的更新

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摘要

Histone acetyltransferases (HATs) and histone deacetylases (HDACs) counteract with each other to regulate gene expression by altering chromatin structure. Aberrant HDAC activity was reported in many human diseases including wide range of cancers, viral infections, cardiovascular complications, auto-immune diseases and kidney diseases. HDAC inhibitors are small molecules designed to block the malignant activity of HDACs. Chemokines and cytokines control inflammation, immunological and other key biological processes and are shown to be involved in various malignancies. Various HDACs and HDAC inhibitors were reported to regulate chemokines and cytokines. Even though HDAC inhibitors have remarkable anti-tumor activity in hematological cancers, they are not effective in treating many diseases and many patients relapse after treatment. However, the role of HDACs and cytokines in regulating these diseases still remain unclear. Therefore, understanding exact mechanisms and effector functions of HDACs are urgently needed to selectively inhibit them and to establish better a platform to combat various malignancies. In this review, we address regulation of chemokines and cytokines by HDACs and HDAC inhibitors and update on HDAC inhibitors in human diseases.
机译:组蛋白乙酰基转移酶(HATs)和组蛋白脱乙酰基酶(HDACs)相互抵消,通过改变染色质结构来调节基因表达。据报道,许多人类疾病中HDAC活性异常,包括广泛的癌症,病毒感染,心血管并发症,自身免疫性疾病和肾脏疾病。 HDAC抑制剂是设计用于阻断HDAC恶性活性的小分子。趋化因子和细胞因子控制炎症,免疫和其他关键生物学过程,并被证明与多种恶性肿瘤有关。据报道,各种HDAC和HDAC抑制剂可调节趋化因子和细胞因子。尽管HDAC抑制剂在血液系统癌症中具有显着的抗肿瘤活性,但它们不能有效治疗多种疾病,许多患者在治疗后复发。但是,HDACs和细胞因子在调节这些疾病中的作用仍然不清楚。因此,迫切需要了解HDAC的确切机制和效应子功能,以选择性地抑制它们并建立更好的平台来对抗各种恶性肿瘤。在这篇综述中,我们探讨了HDAC和HDAC抑制剂对趋化因子和细胞因子的调控,并更新了人类疾病中HDAC抑制剂的情况。

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